Canonical Allele Identifier: CA2625128292
Gene: SIX1 HGNC NCBI

Linked Data

gnomAD v4: 14-60645442-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60645442A>G , CM000676.2:g.60645442A>G GRCh38
NC_000014.8:g.61112160A>G , CM000676.1:g.61112160A>G GRCh37
NC_000014.7:g.60181913A>G NCBI36
NG_008231.1:g.8996T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000645694.3:c.*841T>C MANE Select ENSP00000494686.1:n.*841T>C
ENST00000247182.6:c.*841T>C ENSP00000247182.5:n.*841T>C
ENST00000553535.2:n.1384T>C
ENST00000554986.2:c.*841T>C ENSP00000452700.2:n.*841T>C
ENST00000555955.3:n.2333T>C
NM_005982.3:c.*841T>C NP_005973.1:n.*841T>C
XM_017021602.2:c.*1115T>C XP_016877091.1:n.*1115T>C
NM_005982.4:c.*841T>C MANE Select NP_005973.1:n.*841T>C
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